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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
4 associated genes
No signs/symptoms info
Macrocephaly-autism syndrome
Squamous cell carcinoma of head and neck

PTEN ING1
ING3
PTEN
TNFRSF10B


COMMON
GENES
PTEN



Citations in the biomedical literature:


Macrocephaly-autism syndrome
PTEN
Squamous cell carcinoma of head and neck
ING1 ING3 TNFRSF10B



Macrocephaly-autism syndrome
Squamous cell carcinoma of head and neck

Synonym(s):
(no synonyms)

Synonym(s):
- HNSCC
- Head and neck squamous cell carcinoma

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C535575

No signs/symptoms info available.